Key result
A 7-year-old girl with a deep neck mass was diagnosed with extraskeletal Ewing sarcoma using multimodal imaging and successfully treated with surgical resection, showing no recurrence during follow-up.
Why the study?
What are the imaging characteristics of extraskeletal Ewing sarcoma in a pediatric patient?
Case Report (n=1)
What are the imaging characteristics of extraskeletal Ewing sarcoma in a pediatric patient?
A quick-growing mass in a pediatric patient, even with well-defined margins on imaging, should raise suspicion for a malignant tumor such as extraskeletal Ewing sarcoma.
Pediatric deep-neck EES warrants inclusion in neck-mass differentials; leaves open optimal management pending larger series.
BACKGROUND: Extraskeletal Ewing sarcoma (EES) is a member of the Ewing sarcoma family of tumors which is pathologically known as a small, round, blue cell tumor involving bone and soft tissue. The prevalence of EES is only 15%-25% of all Ewing sarcoma and EES often occurs in patients aged from 20-mo-old to 30-years-old resulting in an unfavorable prognosis. CASE SUMMARY: The present case report described a 7-year-old patient with a palpable EES mass of 33 mm × 27 mm × 28 mm in the deep neck with symptoms of persistent dyspnea over the past 5 mo. After laboratory examinations, abnormal physiological and biochemical indicators were not found. Ultrasound images presented the mass to be complex, solid and fluid-filled with circumscribed margins and posterior acoustic enhancement. The mass also presented with partial internal vascularity. The contrast-enhanced magnetic resonance imaging scan illustrated the outstanding enhancement with fast perfusion mode in the early arterial phase. CONCLUSION: Our study suggested that a quick-growing mass in the pediatric patient is possibly a malignant tumor whether the mass has well-defined margins or not.
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Chen et al. (2022) conducted a case report in Extraskeletal Ewing sarcoma (n=1). Surgical resection was evaluated on Tumor recurrence or metastasis. A 7-year-old girl with a deep neck mass was diagnosed with extraskeletal Ewing sarcoma using multimodal imaging and successfully treated with surgical resection, showing no recurrence during follow-up.
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